Evidence map›Paper›PMID 39316100›Full record

ReviewDer Nervenarzt2025

[Genetic diagnostics of mental health disorders in adulthood].

Laura L Kilarski, Isabelle Claus, Elisabeth B Binder, Franziska Degenhardt, Katharina Domschke, Andreas J Forstner, Hans J Grabe, Urs Heilbronner, Daniel Müller, Markus M Nöthen and 9 more

Abstract readEnglish AbstractReview
In one paragraph

Review in Der Nervenarzt, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Laura L KilarskiKlinik und Poliklinik für Psychiatrie und Psychotherapie, Universitätsklinikum Bonn, Bonn, Deutschland.
Isabelle ClausInstitut für Humangenetik, Universitätsklinikum Bonn, Bonn, Deutschland.
Elisabeth B BinderMax-Planck-Institut für Psychiatrie, Kraepelinstr. 2-10, 80804, München, Deutschland.
Franziska DegenhardtKlinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, LVR-Universitätsklinikum Essen, Kliniken und Institut der Universität Duisburg-Essen, Essen, Deutschland.
Katharina DomschkeKlinik für Psychiatrie und Psychotherapie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Freiburg, Deutschland.
Andreas J ForstnerInstitut für Humangenetik, Universitätsklinikum Bonn, Bonn, Deutschland.
Hans J GrabeKlinik für Psychiatrie und Psychotherapie der Universitätsmedizin Greifswald, Greifswald, Deutschland.
Urs HeilbronnerInstitut für Psychiatrische Phänomik und Genomik (IPPG), LMU Klinikum, LMU München, München, Deutschland.
Daniel MüllerCentre for Addiction and Mental Health, Campbell Family Mental Health Research Institute, Toronto, ON, Kanada.
Markus M NöthenInstitut für Humangenetik, Universitätsklinikum Bonn, Bonn, Deutschland.
Franziska RadtkeKlinik und Poliklinik für Kinder- und Jugendpsychiatrie, Psychosomatik und Psychotherapie, Universitätsklinikum Würzburg, Würzburg, Deutschland.
Marcella RietschelAbteilung für Genetische Epidemiologie in der Psychiatrie, Zentralinstitut für Seelische Gesundheit, Medizinische Fakultät Mannheim, Universität Heidelberg, Mannheim, Deutschland.
Thomas G SchulzeInstitut für Psychiatrische Phänomik und Genomik (IPPG), LMU Klinikum, LMU München, München, Deutschland.
Fabian StreitAbteilung für Psychiatrie und Psychotherapie, Zentralinstitut für Seelische Gesundheit, Medizinische Fakultät Mannheim, Universität Heidelberg, Mannheim, Deutschland.
Ludger Tebartz van ElstKlinik für Psychiatrie und Psychotherapie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Freiburg, Deutschland.
Oliver TüscherZentrum für Seltene Erkrankungen und Klinik für Psychiatrie und Psychotherapie, Universitätsmedizin Mainz, Mainz, Deutschland.
Jürgen DeckertKlinik und Poliklinik für Psychiatrie, Psychosomatik und Psychotherapie, Zentrum für Psychische Gesundheit und Zentrum für Seltene Erkrankungen - Referenzzentrum Nordbayern, Universitätsklinikum Würzburg, Würzburg, Deutschland.
Eva C SchulteKlinik und Poliklinik für Psychiatrie und Psychotherapie, Universitätsklinikum Bonn, Bonn, Deutschland. Eva-Christina.Schulte@ukbonn.de.
das Referat Genetische, Molekulare, Zelluläre Neurowissenschaften der DGPPN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review article provides insights into the role of genetic diagnostics in adult mental health disorders. The importance of genetic factors in the development of mental illnesses, from rare genetic syndromes to common complex genetic disorders, is described. Current clinical characteristics that may warrant a genetic diagnostic work-up are highlighted, including intellectual disability, autism spectrum disorders and severe psychiatric conditions with specific comorbidities, such as organ malformations or epilepsy. The review discusses when genetic diagnostics are recommended according to current guidelines as well as situations where they might be considered even in the absence of explicit guideline recommendations. This is followed by an overview of the procedures and the currently used diagnostic methods. Current limitations and possible developments in the field of genetic diagnostics in psychiatry are discussed, including the fact that, for many mental health conditions, genetic testing is not yet part of standard clinical practice; however, in summary genetic causes should be considered more frequently in certain clinical constellations, and genetic diagnostics and counselling should be offered where appropriate.

Indexed as

Genetic Predisposition to DiseaseGenetic TestingMental DisordersAdultEvidence-Based MedicineGenetic CounselingHumansComplex genetic mental illnessGenetic counsellingGenetic syndromesMental health geneticsPsychiatry

Identifiers

PMID39316100
PMCPMC12254155

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.